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MIS Implants Technologies Ltd.

US

Last updated May 23, 2026

What MIS Implants Technologies Ltd. makes

MIS Implants Technologies Ltd. manufactures dental implant suprastructures, including both permanent and single-use temporary preformed designs. Their portfolio also includes two-piece endosteal dental implants (screw and basket types), reusable surgical procedure kits for dental/maxillofacial procedures, and reusable drill bits for dental fixtures. Additionally, they produce screwing power tool attachments and fluted surgical drill bits for dental applications.

The company’s devices are classified under FDA regulations as Class I and Class II, with products listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does MIS Implants Technologies Ltd. primarily manufacture?

MIS Implants Technologies Ltd. specializes in dental implant-related devices. Their portfolio includes dental implant suprastructures (both permanent and temporary, single-use preformed types), two-piece endosteal dental implants (screw and basket designs), reusable dental/maxillofacial surgical kits, and reusable dental drill bits. They also produce screwing power tool attachments and fluted surgical drill bits for dental applications, focusing on components used in dental restoration and implantology.

Where is MIS Implants Technologies Ltd. based, and how does that affect its regulatory standing?

MIS Implants Technologies Ltd. is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations. The FDA classifies their products as either Class I or Class II, depending on the risk level and intended use, and some of their devices are listed in the FDA’s Unique Device Identifier (UDI) database, which helps track and regulate medical devices in the U.S. market.

Which regulatory registries or databases list MIS Implants Technologies Ltd.’s devices?

MIS Implants Technologies Ltd.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for sale in the United States, ensuring transparency and traceability for healthcare providers and regulators. The inclusion in this database reflects compliance with FDA requirements for device identification and reporting.

How are MIS Implants Technologies Ltd.’s devices classified under FDA regulations?

The FDA categorizes MIS Implants Technologies Ltd.’s devices into Class I or Class II based on their risk levels and intended use. Class I devices generally pose minimal risk and may be exempt from some regulatory controls, while Class II devices require stricter oversight due to moderate risk. For example, reusable surgical kits and drill bits may fall under Class II due to their procedural role in dental surgery, whereas some implant components could be classified as Class I if they present lower risk. The classification determines the regulatory pathway and requirements for authorization.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
514576057

Catalogue (2090)

Page 30 of 42
DeviceModel / ReferenceRegistriesClassStatus
Mis CS-MAB10
FDA UDI
Class IActive
Mis MW-MC102
FDA UDI
Class IIActive
Mis MD-CCI10
FDA UDI
Class IIActive
Mis CG-D0839
FDA UDI
Class IActive
Mis MD-IC040
FDA UDI
Class IActive
Mis 4bone 4B-X2525
FDA UDI
Class IIActive
Mis LNXC-08420
FDA UDI
Class IIActive
Mis CF5C-11500
FDA UDI
Class IIActive
Mis MG-KD06
FDA UDI
Class IActive
Mis MT-TDN19
FDA UDI
Class IActive
Mis MT-IT100
FDA UDI
Class IActive
Mis VN-AT002
FDA UDI
Class IIActive
Mis Seven MF7-06500
FDA UDI
Class IIActive
Mis CW-C2057
FDA UDI
Class IIActive
Mis MK-0049
FDA UDI
Class IActive
Mis LNXC-10330
FDA UDI
Class IIActive
Mis MT-RA480
FDA UDI
Class IActive
Mis CC1-00330
FDA UDI
Class IIActive
Mis MF4-20375
FDA UDI
Class IIActive
Mis MD-S0220
FDA UDI
Class IIActive
Mis Seven MF7-06600
FDA UDI
Class IIActive
Mis Seven MG7-13330
FDA UDI
Class IIActive
Mis C1C-16420
FDA UDI
Class IIActive
Mis CD-SA400
FDA UDI
Class IIActive
Mis EW-IT100
FDA UDI
Class IUnknown
Mis V3C-11390
FDA UDI
Class IIActive
Mis VN-P6340
FDA UDI
Class IIActive
Mis MG-N1124
FDA UDI
Class IActive
MIS Multi Unit MA-AN173
FDA UDI
Class IIActive
Mis MK-SD01
FDA UDI
Class IActive
Mis MT-SMK13
FDA UDI
Class IUnknown
Mis MG-NSI40
FDA UDI
Class IActive
Mis MT-GDM01
FDA UDI
Class IUnknown
Mis CT-BTC45
FDA UDI
Class IActive
Mis MK-CDS08
FDA UDI
Class IActive
Mis CW-IC551
FDA UDI
Class IActive
Mis CK-NLC3
FDA UDI
Class IIActive
Mis CS-HS548
FDA UDI
Class IIActive
Mis VK-CPK81-USA
FDA UDI
Class IIActive
Mis MM-LOCI1
FDA UDI
Class IActive
Mis MT-LBT32
FDA UDI
Class IActive
Mis CS-HS248
FDA UDI
Class IIActive
Mis ED-CPH13
FDA UDI
Class IIUnknown
Mis CN-MAC30
FDA UDI
Class IIActive
Mis EW-CPK82
FDA UDI
Class IIUnknown
Mis MT-PD440
FDA UDI
Class IActive
Mis LT-WSM10
FDA UDI
Class IActive
Mis MG-D1037
FDA UDI
Class IActive
Mis EK-CPK83
FDA UDI
Class IIUnknown
Mis MT-TDN55
FDA UDI
Class IActive

Related Companies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • MIS Implants Technologies Ltd. BAR LEV INDUSTRIAL PARK Northern · IL FEI 3004203816